Publications by authors named "Suat Fitoz"

Introduction: Central tegmental tract hyperintensity (CTTH) on T2-weighted imaging is an uncommon neuroimaging finding in pediatric patients with unclear clinical significance. CTTH may represent either a physiological or pathological process. This study evaluates the relationship between CTTH and MRI sequences (FLAIR, DWI) to explore its diagnostic value.

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  • Developmental anomalies in the cochlea are found in about 25% of individuals with congenital deafness, often with unidentified genetic causes.
  • Researchers used exome sequencing and CRISPR/Cas9 technology to create patient-specific stem cell lines to study the effects of genetic variants related to hearing loss.
  • When differentiating these stem cells into inner ear organoids, the study revealed significant developmental issues in the gene-edited lines, demonstrating the potential of organoids to validate the effects of genetic variants linked to cochlear malformations.
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  • Carpal tunnel syndrome (CTS) in children is often caused by mucopolysaccharidosis (MPS), and this study explores using wrist ultrasonography (US) as an alternative diagnostic method to traditional electrophysiological tests.
  • The study involved 27 MPS patients and 30 healthy controls, revealing that 30 out of 54 wrists in the MPS group were diagnosed with CTS, with specific measurements showing higher values in affected individuals compared to controls.
  • While the ultrasonography results showed some limitations in specificity and sensitivity, it remains a promising noninvasive diagnostic technique for CTS, especially using the wrist-forearm ratio (WFR) for analysis.
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Traumatic brain injury (TBI) is a leading cause of morbidity and mortality in children. Head computed tomography (CT) is frequently utilized for evaluating trauma-related characteristics, selecting treatment options, and monitoring complications in the early stages. This study assessed the relationship between cranial CT findings and early and late neurological outcomes in pediatric TBI patients admitted to the pediatric intensive care unit (PICU).

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Background: Nutcracker syndrome (NCS) describes a set of symptoms and signs resulting from compression of the left renal vein (LRV). There is a lack of knowledge about its natural course, diagnosis, and management, especially in children. Herein, we present our single-center experience with a large number of patients who have long-term follow-up results.

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Background: Liver transplantation (LT) is a well-established, life-saving treatment for children with irreversible acute and chronic liver failure (LF). We aimed to evaluate the factors associated with morbidity and mortality in the early period of LT in children by reviewing our pediatric intensive care unit (PICU) experience.

Methods: We reviewed children`s medical records followed in the PICU after LT between May 2015-August 2021, including demographic parameters, indications for LT, operative variables, respiratory and circulatory support requirements, LT-related complications and survival.

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Objective: The aims of this study were to describe disease associations of magnetic resonance imaging (MRI)-confirmed and clinically symptomatic sacroiliitis in pediatric patients with rheumatic diseases and to examine the relationship between patient characteristics and MRI findings of the sacroiliac joint (SIJ).

Methods: Demographic and clinical data were extracted from the electronic medical records of the patients with sacroiliitis followed in the last 5 years. Active inflammatory and structural damage lesions of the SIJ-MRI were examined by the modified Spondyloarthritis Research Consortium of Canada scoring system, and correlation analysis of these results with clinical characteristics was evaluated.

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The current study aimed to investigate the clinical, laboratory and radiological findings of the pneumonia cases in children that were confirmed as M.pneumoniae by polymerase chain reaction (PCR) testing and to reveal the factors that can be decisive in the diagnosis. Seventy-seven children were included in this study.

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Invasive aspergillosis (IA) is a major cause of morbidity and mortality. This study aimed to present our 10-year IA experience at a single center. Fifty-nine pediatric patients with IA were included in this study.

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  • - The study investigates early cranial MRI findings in newborns suspected of having inborn metabolic disorders (IMDs), focusing on identifying specific neuroimaging patterns.
  • - Out of 195 infants screened, 56 had cranial MRI scans within three months, revealing that those diagnosed with IMDs showed significantly higher T2-hyperintensity in white matter and basal ganglia compared to those not diagnosed.
  • - Early neuroimaging is crucial for diagnosing IMDs, emphasizing the need for healthcare professionals to understand these findings, particularly in areas without advanced neonatal screening programs.
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Purpose: The purpose of the study is to evaluate MRI findings of middle fossa arachnoid cysts in children according to Galassi classification and determine the differences between types and to assess the morphological changes in cysts during follow-up imaging.

Methods: MR images of 266 middle fossa arachnoid cysts of 255 pediatric patients were evaluated by two experienced radiologists retrospectively. MRI features including the sidedness of the cyst, Galassi type, parenchymal compression findings (cortical flattening and white matter compression), bone remodeling, and midline shift were evaluated on axial T2- and T1-weighted images.

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Objective: The aim of this study is to analyze the clinical features, neuroimaging findings and outcomes of the children admitted to our tertiary pediatric intensive care unit (PICU) due to posterior reversible encephalopathy syndrome (PRES).

Methods: This was a retrospective study where the hospital records of children admitted to PICU due to PRES between January 1, 2011 and January 1, 2021 were reviewed.

Results: We enrolled 14 patients with a median age of 8 years (IQR 2.

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Background: Magnetic resonance imaging (MRI) is often the first modality of choice in the detection of pituitary pathologies due to its excellent contrast resolution and high spatial resolution. However, evaluating the size of the pituitary gland is somewhat difficult since the gland morphology varies widely among individuals.

Objective: The aim of this study was to provide normal reference values for pituitary volumes in the pediatric population using three-dimensional (3-D) MRI data.

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The clinical manifestations of SARS-CoV-2 infection mainly involve the respiratory system. However, there is increasing evidence that this virus can affect other organs, causing a wide range of clinical symptoms. This is the report of a 40-day-old patient who presented with sepsis and had no risk factors other than SARS-CoV-2 infection, whose radiological findings were compatible with cerebral sinus vein thrombosis.

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Purpose: Many diseases of traumatic, infectious, endocrinologic and neoplastic origin can lead to orbital involvement and related morphological changes. In the present study, we aimed to determine the age-based normal orbital measurements using magnetic resonance imaging (MRI) in pediatric patients.

Methods: Our retrospective study included 186 patients with normal orbital MRI findings.

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Objectives: Appendicitis is a common surgical emergency among children. The coronavirus pandemic affected the system of hospitals more than any other field, and great amount of people were concerned about visiting the hospitals for any reason. In this study, it was aimed to evaluate the profile of appendicitis by emphasizing perforated and acute appendicitis in the pandemic period and to compare the rates with previous three years.

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Objective: Bladder wall thickness (BWTh) measurements and Nerve Growth Factor (NGF) /creatinine (Cr) values, as noninvasive tools, were found to predict daytime voiding problems in children with overactive bladder (OAB). The goal of this research was to examine if bladder wall thickness together with urine NGF/Cr could be a clinical utility in treatment outcome of OAB in children.

Patients And Methods: A total of 60 children with OAB, (Group 1; n=40) and healthy normal controls (Group 2; n=20), aged 6-14 years old were involved in this prospective study.

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Background: Invasive aspergillosis (IA) is an important cause of morbidity and mortality in immunosuppressed children. Early detection of the infection can improve prognosis in this patient population.

Objectives: To investigate the utility of galactomannan antigen assay (GM-EIA) as a diagnostic tool for IA in at-risk paediatric patients.

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Introduction: Familial Mediterranean fever (FMF) is the most common hereditary autoinflammatory disease with an increased risk for secondary amyloidosis. Since lifelong colchicine has been the treatment of choice that prevents renal amyloidosis, non-amyloid kidney diseases are more frequently considered in the differential diagnosis of proteinuria. Nutcracker syndrome (NCS) can be one of the confounding causes.

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Background: Systemic lupus erythematous (SLE) is extremely rare in infants and has been reported to be a much more severe disease with higher prevalence of critical organ involvement. Herein we present the clinical and laboratory features of infantile SLE (iSLE) with an onset of nephrotic syndrome (NS) during the first year of life.

Case: A 12-month-old boy was suffering from generalized edema for two months.

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A 2-year-old boy was referred to the Ankara University School of Medicine Children's Hospital with a history of recurrent respiratory distress and cyanosis since birth. His medical history was significant for premature birth at 31 weeks via cesarean section, as an infant of a diabetic mother. There was no parental consanguinity.

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